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Collect. Czech. Chem. Commun. 1994, 59, 2641-2649
https://doi.org/10.1135/cccc19942641

Phenanthridinium-Based Azomethine Ylides in 1,3-Dipolar Cycloaddition with Dimethyl Acetylenedicarboxylate

Milan Potáčeka, Tomáš Topinkaa, Jiří Dostálb and Jaromír Marekc

a Department of Organic Chemistry, Masaryk University, 611 37 Brno, Czech Republic
b Department of Biochemistry, Masaryk University, 662 43 Brno, Czech Republic
c Department of Inorganic Chemistry, Masaryk University, 611 37 Brno, Czech Republic

Crossref Cited-by Linking

  • Ito S., Tokimaru Y., Nozaki K.: Isoquinolino[4,3,2-de]phenanthridine: synthesis and its use in 1,3-dipolar cycloadditions to form nitrogen-containing polyaromatic hydrocarbons. Chem. Commun. 2015, 51, 221. <https://doi.org/10.1039/C4CC06643J>
  • Mehrabi Hossein, Pishahang Jaleh: Efficient Synthesis of Pyrrolo[1,2-f]phenanthridine Derivatives via Dipolar Cycloaddition of Phenanthridine, Activated Acetylenes, and Ethyl Bromopyruvate. Synthetic Communications 2014, 44, 76. <https://doi.org/10.1080/00397911.2013.789525>
  • Travnicek Martin, Potácek Milan, Mannschreck Albrecht: STEREOCHEMISTRY OF 1,3-DIPOLAR CYCLOADDITION REACTION OF AZOMETHINE YLIDES DERIVED FROM N-ALKYL-N-(4-TOLUENESULPHONYL) CARBAMOYLMETHYL PHENANTHRIDINIUM WITH OLEFINIC DIPOLAROPHILES. Heterocyclic Communications 2001, 7. <https://doi.org/10.1515/HC.2001.7.3.213>
  • POTACEK M., TOPINKA T., DOSTAL J., MAREK J.: ChemInform Abstract: Phenanthridinium‐Based Azomethine Ylides in 1,3‐Dipolar Cycloaddition with Dimethyl Acetylenedicarboxylate. ChemInform 1995, 26. <https://doi.org/10.1002/chin.199523148>
  • Temciuc Ecaterina, Hornfeldt Anna-Britta, Gronowitz Salo, Stlhandske Claes: An unexpected [2+2]-cycloaddition reaction of 4-methyldithieno-[3,4-b:3′,2′-d]pyridinium iodide with dimethyl acetylenedicarboxylate. Tetrahedron 1995, 51, 13185. <https://doi.org/10.1016/0040-4020(95)00789-B>